Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/13750
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dc.contributor.authorGeorgakilas, V.en
dc.contributor.authorGournis, D.en
dc.contributor.authorBourlinos, A. B.en
dc.contributor.authorKarakassides, M. A.en
dc.contributor.authorPetridis, D.en
dc.date.accessioned2015-11-24T17:32:34Z-
dc.date.available2015-11-24T17:32:34Z-
dc.identifier.issn0947-6539-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/13750-
dc.rightsDefault Licence-
dc.subjectclaysen
dc.subjectintercalationsen
dc.subjectmacrocyclesen
dc.subjectsupramolecular chemistryen
dc.subjecttemplate synthesisen
dc.subjectcatalystsen
dc.subjectmontmorilloniteen
dc.subjectrotaxanesen
dc.titleClays as a host matrix in the synthesis of organic macrocyclesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1002/chem.200204555-
heal.identifier.secondary<Go to ISI>://000184925700021-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Μηχανικών Επιστήμης Υλικώνel
heal.publicationDate2003-
heal.abstractA new approach for the synthesis of amide macrocycles, based on the use of organo-clay derivatives as controlling template, is proposed as an alternative to the rotaxane method. Dications of p-xylylene diamine inserted in the clay interlayer space act as molding pillars around which neutral diamine molecules are erected via hydrogen bonding and pi - pi interactions to form supramolecular arrays. Condensation of diamines in the supramolecular arrays with diacetyl dichlorides yields various tetramide macrocycles in good yields. Shape, aromaticity and dimensions of the reactants are factors affecting the condensation reaction.en
heal.publisherWiley-VCH Verlagen
heal.journalNameChemistry-a European Journalen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

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